Nifedipine
NDC 51655-798, Nifedipine, tablet, extended release, from Northwind Health Company, LLC.
- Product NDC
- 51655-798
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075269
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51655-798 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NIFEDIPINE30 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51655-798-26 | 51655079826 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-798-26) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/d9dec600-4e11-8292-e053-2a95a90a6842
Use it
Look up 51655-798 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-798 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-798. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.